AI Article Synopsis

  • A series of ternary HfTiO and TiAlO films, along with quaternary HfTiAlO films, were deposited using atomic layer deposition on silicon substrates to explore their electrical performance in metal-oxide-semiconductor capacitors.
  • The study found that increasing Ti in HfTiO improved permittivity but led to increased leakage current, while increasing Al in TiAlO improved interface quality at the cost of permittivity.
  • HfTiAlO films with a specific cycle ratio (Hf:Ti:Al = 6:1:1) achieved the best overall performance, with a high dielectric constant, improved conduction band offset with silicon, and the lowest leakage current density.

Article Abstract

In this work, a series of ternary HfTiO and TiAlO films and quaternary HfTiAlO films prepared with different stoichiometric ratios atomic layer deposition (ALD) were deposited on Si substrates. The interfacial properties, band alignments, and electrical characteristics were analyzed to evaluate the electrical performance of the corresponding metal-oxide-semiconductor (MOS) capacitors. Based on the characterization data, it can be noted that the permittivity of HfTiO increases on increasing the Ti content, while the deterioration of the film quality leads to an increased leakage current. For TiAlO, as the Al content increased gradually, the interface quality improved, but the corresponding permittivity was sacrificed. As for HfTiAlO, the addition of Ti and Al jointly in HfO could improve the interface performance, enlarge the energy band offset, enhance the dielectric constant, and reduce the leakage current simultaneously. The interfacial analysis and electrical characterization demonstrated that HfTiAlO with an ALD cycle ratio of Hf : Ti : Al = 6 : 1 : 1 had the most excellent film quality, interface performance and electrical properties, including a larger dielectric constant of 28.8, a larger conduction band offset with Si of 2.47 eV, and the lowest leakage current density of 1.11 × 10 A cm.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052381PMC
http://dx.doi.org/10.1039/d0ra01073aDOI Listing

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